Prescription drug · UNAPPROVED DRUG OTHER
Diclolidol Kit (Lidocaine hcl, diclofenac sodium) NDC 59088-806
Kit · PureTek Corporation
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 59088-806-00 | 5908808060059088080600 | 1 KIT in 1 KIT (59088-806-00) * 85 g in 1 BOTTLE, WITH APPLICATOR (59088-327-07) * 1 TUBE in 1 CARTON (43598-977-10) / 100 g in 1 TUBEMarketed from Sep 9, 2025 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Diclolidol Kit
- Generic name (nonproprietary)
- lidocaine hcl, diclofenac sodium
- Dosage form
- Kit
- Labeler
- PureTek CorporationNDC labeler code 59088
- Product type
- Prescription drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- Identifiers
- Product ID 59088-806_3e63324b-e762-9367-e063-6394a90a2981SPL ID 3e63324b-e762-9367-e063-6394a90a2981SPL set ID 3e63324b-e761-9367-e063-6394a90a2981RxCUI 855633, 1010057UPC 0359088806005
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.
- NDC on a medical claim
N459088080600followed by a unit qualifier and the quantityPackage 59088-0806-00. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Indications: For the temporary relief of arthritis pain ONLY in the following areas: hand, wrist, elbow (upper body areas) foot, ankle, knee (lower body areas) this product may take up to 7 days to work for arthritis pain; it is not for immediate relief. If no pain relief in 7 days, stop use. Directions: These highlights do not include all the information needed to use Diclofenac Sodium 1% Topical Gel safely and effectively. See full prescribing information for Diclofenac Sodium 1% Topical Gel. Initial U.S. Approval: 1988 Use up to 21 days unless directed by your doctor Not for strains, sprains, bruises or sports injuries. This product has not been shown to work for these types of injuries. …
Excerpt only. Read the full label for complete information.
About NDC 59088-806
- What is NDC 59088-806?
- 59088-806 is the product NDC for Diclolidol Kit kit, listed with the FDA by PureTek Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Diclolidol Kit (Lidocaine HCl, Diclofenac Sodium).
- Who is the labeler?
- PureTek Corporation, NDC labeler code 59088. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Diclolidol Kit?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.